Incidental Mutation 'R8803:Cad'
ID |
671610 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cad
|
Ensembl Gene |
ENSMUSG00000013629 |
Gene Name |
carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase |
Synonyms |
2410008J01Rik |
MMRRC Submission |
068640-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.968)
|
Stock # |
R8803 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
5 |
Chromosomal Location |
31212124-31235823 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to G
at 31226908 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Alanine
at position 1222
(S1222A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000013773
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000013773]
[ENSMUST00000200953]
[ENSMUST00000201182]
[ENSMUST00000201838]
[ENSMUST00000202795]
[ENSMUST00000202973]
|
AlphaFold |
B2RQC6 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000013773
AA Change: S1222A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000013773 Gene: ENSMUSG00000013629 AA Change: S1222A
Domain | Start | End | E-Value | Type |
CPSase_sm_chain
|
1 |
139 |
8.81e-80 |
SMART |
Pfam:GATase
|
179 |
356 |
4.7e-47 |
PFAM |
low complexity region
|
397 |
407 |
N/A |
INTRINSIC |
Pfam:ATP-grasp_4
|
511 |
692 |
1.2e-15 |
PFAM |
Pfam:CPSase_L_D2
|
514 |
718 |
1.8e-85 |
PFAM |
Pfam:ATP-grasp
|
522 |
690 |
1.5e-9 |
PFAM |
Pfam:Dala_Dala_lig_C
|
527 |
687 |
2.2e-10 |
PFAM |
CPSase_L_D3
|
798 |
921 |
9.7e-59 |
SMART |
Pfam:ATP-grasp_4
|
1044 |
1223 |
1.8e-23 |
PFAM |
Pfam:CPSase_L_D2
|
1047 |
1250 |
3.1e-28 |
PFAM |
Pfam:Dala_Dala_lig_C
|
1054 |
1242 |
2.3e-7 |
PFAM |
Pfam:ATP-grasp
|
1055 |
1222 |
2.1e-12 |
PFAM |
MGS
|
1327 |
1428 |
1.35e-7 |
SMART |
Pfam:Amidohydro_1
|
1462 |
1730 |
7.4e-12 |
PFAM |
low complexity region
|
1820 |
1839 |
N/A |
INTRINSIC |
low complexity region
|
1864 |
1880 |
N/A |
INTRINSIC |
Pfam:OTCace_N
|
1924 |
2065 |
1.9e-44 |
PFAM |
Pfam:OTCace
|
2071 |
2221 |
7.6e-37 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000200953
AA Change: S1159A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000144307 Gene: ENSMUSG00000013629 AA Change: S1159A
Domain | Start | End | E-Value | Type |
CPSase_sm_chain
|
1 |
139 |
8.81e-80 |
SMART |
Pfam:GATase
|
179 |
356 |
4.5e-47 |
PFAM |
low complexity region
|
397 |
407 |
N/A |
INTRINSIC |
Pfam:CPSase_L_D2
|
514 |
616 |
1.5e-34 |
PFAM |
Pfam:Dala_Dala_lig_C
|
527 |
625 |
2.4e-7 |
PFAM |
Pfam:CPSase_L_D2
|
614 |
655 |
4.9e-15 |
PFAM |
CPSase_L_D3
|
735 |
858 |
9.7e-59 |
SMART |
Pfam:ATP-grasp_4
|
981 |
1160 |
1.7e-23 |
PFAM |
Pfam:CPSase_L_D2
|
984 |
1187 |
3e-28 |
PFAM |
Pfam:Dala_Dala_lig_C
|
991 |
1179 |
2.3e-7 |
PFAM |
Pfam:ATP-grasp
|
992 |
1159 |
2.1e-12 |
PFAM |
MGS
|
1264 |
1365 |
1.35e-7 |
SMART |
Pfam:Amidohydro_1
|
1399 |
1667 |
7.1e-12 |
PFAM |
low complexity region
|
1757 |
1776 |
N/A |
INTRINSIC |
low complexity region
|
1801 |
1817 |
N/A |
INTRINSIC |
Pfam:OTCace_N
|
1861 |
2002 |
1.8e-44 |
PFAM |
Pfam:OTCace
|
2008 |
2158 |
7.3e-37 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000201182
AA Change: S1222A
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000144684 Gene: ENSMUSG00000013629 AA Change: S1222A
Domain | Start | End | E-Value | Type |
CPSase_sm_chain
|
1 |
139 |
8.81e-80 |
SMART |
Pfam:GATase
|
179 |
356 |
4.5e-47 |
PFAM |
low complexity region
|
397 |
407 |
N/A |
INTRINSIC |
Pfam:ATP-grasp_4
|
511 |
692 |
1.1e-15 |
PFAM |
Pfam:CPSase_L_D2
|
514 |
718 |
1.7e-85 |
PFAM |
Pfam:ATP-grasp
|
522 |
690 |
1.4e-9 |
PFAM |
Pfam:Dala_Dala_lig_C
|
527 |
687 |
2.1e-10 |
PFAM |
CPSase_L_D3
|
798 |
921 |
9.7e-59 |
SMART |
Pfam:ATP-grasp_4
|
1044 |
1223 |
1.7e-23 |
PFAM |
Pfam:CPSase_L_D2
|
1047 |
1250 |
3e-28 |
PFAM |
Pfam:Dala_Dala_lig_C
|
1054 |
1242 |
2.3e-7 |
PFAM |
Pfam:ATP-grasp
|
1055 |
1222 |
2.1e-12 |
PFAM |
MGS
|
1327 |
1428 |
1.35e-7 |
SMART |
Pfam:Amidohydro_1
|
1462 |
1730 |
7.1e-12 |
PFAM |
low complexity region
|
1820 |
1839 |
N/A |
INTRINSIC |
low complexity region
|
1864 |
1880 |
N/A |
INTRINSIC |
Pfam:OTCace_N
|
1949 |
1994 |
1.4e-11 |
PFAM |
Pfam:OTCace
|
2000 |
2150 |
7.3e-37 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000201838
|
SMART Domains |
Protein: ENSMUSP00000144127 Gene: ENSMUSG00000013629
Domain | Start | End | E-Value | Type |
CPSase_sm_chain
|
1 |
139 |
8.81e-80 |
SMART |
Pfam:GATase
|
179 |
356 |
6.3e-48 |
PFAM |
low complexity region
|
397 |
407 |
N/A |
INTRINSIC |
Pfam:ATP-grasp_4
|
511 |
692 |
1.9e-16 |
PFAM |
Pfam:CPSase_L_D2
|
514 |
718 |
3.7e-86 |
PFAM |
Pfam:ATP-grasp
|
522 |
690 |
2.5e-10 |
PFAM |
Pfam:Dala_Dala_lig_C
|
526 |
687 |
4.2e-11 |
PFAM |
CPSase_L_D3
|
798 |
921 |
9.7e-59 |
SMART |
SCOP:d1a9xa3
|
935 |
964 |
1e-7 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000202795
AA Change: S1222A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000144009 Gene: ENSMUSG00000013629 AA Change: S1222A
Domain | Start | End | E-Value | Type |
CPSase_sm_chain
|
1 |
139 |
8.81e-80 |
SMART |
Pfam:GATase
|
179 |
356 |
1.9e-47 |
PFAM |
low complexity region
|
397 |
407 |
N/A |
INTRINSIC |
Pfam:ATP-grasp_4
|
511 |
692 |
5.9e-16 |
PFAM |
Pfam:CPSase_L_D2
|
514 |
718 |
1.2e-85 |
PFAM |
Pfam:ATP-grasp
|
522 |
690 |
7.3e-10 |
PFAM |
Pfam:Dala_Dala_lig_C
|
527 |
687 |
1.3e-10 |
PFAM |
CPSase_L_D3
|
798 |
921 |
9.7e-59 |
SMART |
Pfam:ATP-grasp_4
|
1044 |
1223 |
8.9e-24 |
PFAM |
Pfam:CPSase_L_D2
|
1047 |
1250 |
2.1e-28 |
PFAM |
Pfam:Dala_Dala_lig_C
|
1054 |
1242 |
1.3e-7 |
PFAM |
Pfam:ATP-grasp
|
1055 |
1222 |
1.1e-12 |
PFAM |
MGS
|
1327 |
1428 |
1.35e-7 |
SMART |
Pfam:Amidohydro_1
|
1462 |
1730 |
2.5e-11 |
PFAM |
low complexity region
|
1820 |
1839 |
N/A |
INTRINSIC |
low complexity region
|
1864 |
1880 |
N/A |
INTRINSIC |
Pfam:OTCace_N
|
1970 |
2004 |
4.6e-11 |
PFAM |
Pfam:OTCace
|
2010 |
2160 |
9.9e-37 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000202973
|
SMART Domains |
Protein: ENSMUSP00000144679 Gene: ENSMUSG00000013629
Domain | Start | End | E-Value | Type |
SCOP:d1gkra1
|
1 |
84 |
4e-28 |
SMART |
PDB:4C6N|A
|
1 |
119 |
4e-58 |
PDB |
low complexity region
|
156 |
170 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
Validation Efficiency |
100% (68/68) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The de novo synthesis of pyrimidine nucleotides is required for mammalian cells to proliferate. This gene encodes a trifunctional protein which is associated with the enzymatic activities of the first 3 enzymes in the 6-step pathway of pyrimidine biosynthesis: carbamoylphosphate synthetase (CPS II), aspartate transcarbamoylase, and dihydroorotase. This protein is regulated by the mitogen-activated protein kinase (MAPK) cascade, which indicates a direct link between activation of the MAPK cascade and de novo biosynthesis of pyrimidine nucleotides. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
T |
A |
8: 60,998,290 (GRCm39) |
S431T |
probably benign |
Het |
Acot7 |
T |
G |
4: 152,302,272 (GRCm39) |
V128G |
probably damaging |
Het |
Actn3 |
T |
C |
19: 4,914,691 (GRCm39) |
D508G |
probably benign |
Het |
Adam18 |
T |
C |
8: 25,137,878 (GRCm39) |
I321V |
probably benign |
Het |
Ak1 |
T |
C |
2: 32,523,490 (GRCm39) |
V186A |
probably benign |
Het |
Aldh3a2 |
A |
G |
11: 61,139,756 (GRCm39) |
F459L |
probably benign |
Het |
Atp11a |
T |
C |
8: 12,875,721 (GRCm39) |
L256P |
probably benign |
Het |
Bcan |
T |
C |
3: 87,903,999 (GRCm39) |
E162G |
probably benign |
Het |
Birc6 |
A |
G |
17: 74,959,033 (GRCm39) |
Q3850R |
probably damaging |
Het |
Btf3l4 |
T |
G |
4: 108,689,084 (GRCm39) |
|
probably benign |
Het |
Btla |
A |
G |
16: 45,059,430 (GRCm39) |
T45A |
probably benign |
Het |
Cbarp |
A |
G |
10: 79,972,976 (GRCm39) |
V39A |
possibly damaging |
Het |
Cct2 |
A |
C |
10: 116,894,090 (GRCm39) |
D221E |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,177,991 (GRCm39) |
D3621G |
probably damaging |
Het |
Col20a1 |
G |
T |
2: 180,643,131 (GRCm39) |
R867L |
possibly damaging |
Het |
Cops3 |
A |
G |
11: 59,718,802 (GRCm39) |
V164A |
probably benign |
Het |
Crygf |
A |
G |
1: 65,967,148 (GRCm39) |
R91G |
probably damaging |
Het |
Csmd2 |
T |
A |
4: 128,440,477 (GRCm39) |
S3181T |
|
Het |
Cyb5r1 |
G |
T |
1: 134,333,696 (GRCm39) |
|
probably benign |
Het |
Dennd6b |
T |
A |
15: 89,070,383 (GRCm39) |
I429F |
probably benign |
Het |
Dock1 |
A |
G |
7: 134,475,816 (GRCm39) |
T864A |
probably benign |
Het |
Eea1 |
A |
T |
10: 95,859,853 (GRCm39) |
D713V |
probably benign |
Het |
Fam78b |
G |
A |
1: 166,829,160 (GRCm39) |
C9Y |
probably damaging |
Het |
Gga2 |
A |
C |
7: 121,597,002 (GRCm39) |
D371E |
probably benign |
Het |
Gtpbp6 |
A |
T |
5: 110,255,186 (GRCm39) |
V2E |
unknown |
Het |
Hectd4 |
A |
T |
5: 121,461,994 (GRCm39) |
M954L |
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,610,248 (GRCm39) |
C1474R |
probably damaging |
Het |
Igkv1-99 |
G |
T |
6: 68,519,370 (GRCm39) |
G109V |
|
Het |
Izumo3 |
T |
C |
4: 92,033,310 (GRCm39) |
|
probably null |
Het |
Kremen1 |
T |
C |
11: 5,144,981 (GRCm39) |
D465G |
probably benign |
Het |
Ksr1 |
T |
C |
11: 79,036,882 (GRCm39) |
E75G |
probably benign |
Het |
Mmp17 |
G |
T |
5: 129,675,773 (GRCm39) |
E311* |
probably null |
Het |
Mmrn1 |
T |
A |
6: 60,965,271 (GRCm39) |
F1101I |
probably damaging |
Het |
Muc13 |
G |
A |
16: 33,633,287 (GRCm39) |
|
probably benign |
Het |
Myl4 |
T |
A |
11: 104,475,403 (GRCm39) |
M147K |
probably damaging |
Het |
Myo1a |
T |
A |
10: 127,546,856 (GRCm39) |
N334K |
probably benign |
Het |
Myo3b |
T |
C |
2: 70,083,338 (GRCm39) |
S664P |
probably benign |
Het |
Nptxr |
T |
C |
15: 79,678,655 (GRCm39) |
N211D |
probably damaging |
Het |
Ntf5 |
A |
G |
7: 45,065,485 (GRCm39) |
T206A |
probably benign |
Het |
Obscn |
T |
A |
11: 58,945,229 (GRCm39) |
E4596D |
probably benign |
Het |
Or4d10c |
T |
C |
19: 12,065,469 (GRCm39) |
E229G |
probably benign |
Het |
Or4f14d |
T |
C |
2: 111,960,427 (GRCm39) |
H243R |
probably damaging |
Het |
Or5ak20 |
T |
A |
2: 85,184,078 (GRCm39) |
Q64L |
probably damaging |
Het |
Or5ak25 |
T |
A |
2: 85,268,981 (GRCm39) |
I174F |
probably damaging |
Het |
Or5b3 |
A |
T |
19: 13,388,037 (GRCm39) |
I35F |
probably damaging |
Het |
Or7e169 |
A |
T |
9: 19,757,462 (GRCm39) |
I151N |
possibly damaging |
Het |
Paip2 |
A |
G |
18: 35,749,273 (GRCm39) |
N114D |
possibly damaging |
Het |
Pcnx1 |
T |
C |
12: 82,039,925 (GRCm39) |
S2071P |
possibly damaging |
Het |
Pcsk2 |
A |
G |
2: 143,637,870 (GRCm39) |
T369A |
probably damaging |
Het |
Ppp1r12b |
A |
C |
1: 134,818,492 (GRCm39) |
|
probably benign |
Het |
Ppp1r35 |
T |
A |
5: 137,777,731 (GRCm39) |
D132E |
possibly damaging |
Het |
Pramel7 |
A |
T |
2: 87,320,405 (GRCm39) |
V296E |
probably benign |
Het |
Prh1 |
C |
T |
6: 132,548,948 (GRCm39) |
P152S |
unknown |
Het |
Pygl |
T |
C |
12: 70,242,390 (GRCm39) |
T689A |
probably damaging |
Het |
Rasgef1b |
T |
C |
5: 99,369,269 (GRCm39) |
S450G |
probably benign |
Het |
Rtn4ip1 |
G |
T |
10: 43,783,842 (GRCm39) |
R121L |
probably damaging |
Het |
Scarf2 |
A |
T |
16: 17,620,695 (GRCm39) |
H121L |
probably damaging |
Het |
Selenbp1 |
C |
A |
3: 94,851,821 (GRCm39) |
A454E |
possibly damaging |
Het |
Slc7a9 |
A |
G |
7: 35,163,143 (GRCm39) |
I449M |
possibly damaging |
Het |
Snapc2 |
C |
T |
8: 4,305,558 (GRCm39) |
H278Y |
probably damaging |
Het |
Stambp |
C |
T |
6: 83,524,212 (GRCm39) |
|
probably null |
Het |
Syne1 |
T |
C |
10: 5,311,535 (GRCm39) |
Y550C |
probably damaging |
Het |
Tas2r113 |
T |
C |
6: 132,870,104 (GRCm39) |
V44A |
possibly damaging |
Het |
Trpv4 |
T |
C |
5: 114,772,816 (GRCm39) |
T305A |
probably benign |
Het |
Twf1 |
T |
C |
15: 94,479,136 (GRCm39) |
Y241C |
probably damaging |
Het |
Ugt2a3 |
T |
C |
5: 87,484,389 (GRCm39) |
K212E |
probably damaging |
Het |
Ush2a |
A |
T |
1: 188,676,998 (GRCm39) |
H4770L |
probably benign |
Het |
Zfc3h1 |
T |
C |
10: 115,247,800 (GRCm39) |
V1001A |
probably benign |
Het |
Zfp335 |
C |
T |
2: 164,751,290 (GRCm39) |
R92Q |
probably benign |
Het |
|
Other mutations in Cad |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00821:Cad
|
APN |
5 |
31,218,828 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00908:Cad
|
APN |
5 |
31,216,398 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01068:Cad
|
APN |
5 |
31,219,114 (GRCm39) |
splice site |
probably benign |
|
IGL01638:Cad
|
APN |
5 |
31,224,958 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02483:Cad
|
APN |
5 |
31,218,170 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02499:Cad
|
APN |
5 |
31,226,948 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02691:Cad
|
APN |
5 |
31,212,638 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03002:Cad
|
APN |
5 |
31,212,330 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4696001:Cad
|
UTSW |
5 |
31,229,438 (GRCm39) |
missense |
probably damaging |
0.99 |
R0212:Cad
|
UTSW |
5 |
31,235,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R0317:Cad
|
UTSW |
5 |
31,229,665 (GRCm39) |
missense |
probably benign |
0.01 |
R0335:Cad
|
UTSW |
5 |
31,231,329 (GRCm39) |
unclassified |
probably benign |
|
R0401:Cad
|
UTSW |
5 |
31,231,330 (GRCm39) |
unclassified |
probably benign |
|
R0445:Cad
|
UTSW |
5 |
31,230,053 (GRCm39) |
missense |
probably benign |
0.08 |
R0494:Cad
|
UTSW |
5 |
31,234,856 (GRCm39) |
unclassified |
probably benign |
|
R0532:Cad
|
UTSW |
5 |
31,219,531 (GRCm39) |
splice site |
probably benign |
|
R0539:Cad
|
UTSW |
5 |
31,232,801 (GRCm39) |
splice site |
probably benign |
|
R0578:Cad
|
UTSW |
5 |
31,216,120 (GRCm39) |
missense |
probably benign |
0.01 |
R0590:Cad
|
UTSW |
5 |
31,219,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R0638:Cad
|
UTSW |
5 |
31,235,032 (GRCm39) |
missense |
probably damaging |
0.98 |
R0831:Cad
|
UTSW |
5 |
31,224,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R1329:Cad
|
UTSW |
5 |
31,216,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Cad
|
UTSW |
5 |
31,226,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R1531:Cad
|
UTSW |
5 |
31,233,563 (GRCm39) |
missense |
probably benign |
0.14 |
R1763:Cad
|
UTSW |
5 |
31,218,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Cad
|
UTSW |
5 |
31,215,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R1786:Cad
|
UTSW |
5 |
31,215,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Cad
|
UTSW |
5 |
31,215,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R2165:Cad
|
UTSW |
5 |
31,219,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R3103:Cad
|
UTSW |
5 |
31,219,018 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3113:Cad
|
UTSW |
5 |
31,231,481 (GRCm39) |
missense |
possibly damaging |
0.50 |
R3762:Cad
|
UTSW |
5 |
31,232,890 (GRCm39) |
splice site |
probably null |
|
R3847:Cad
|
UTSW |
5 |
31,218,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R3898:Cad
|
UTSW |
5 |
31,231,366 (GRCm39) |
missense |
probably benign |
0.06 |
R3943:Cad
|
UTSW |
5 |
31,229,729 (GRCm39) |
critical splice donor site |
probably null |
|
R4213:Cad
|
UTSW |
5 |
31,229,688 (GRCm39) |
missense |
probably benign |
0.01 |
R4458:Cad
|
UTSW |
5 |
31,218,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R4562:Cad
|
UTSW |
5 |
31,215,477 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4629:Cad
|
UTSW |
5 |
31,227,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R4717:Cad
|
UTSW |
5 |
31,224,030 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4811:Cad
|
UTSW |
5 |
31,232,034 (GRCm39) |
missense |
probably benign |
0.02 |
R5044:Cad
|
UTSW |
5 |
31,212,365 (GRCm39) |
missense |
probably benign |
0.00 |
R5630:Cad
|
UTSW |
5 |
31,217,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R5660:Cad
|
UTSW |
5 |
31,234,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R6008:Cad
|
UTSW |
5 |
31,226,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R6029:Cad
|
UTSW |
5 |
31,212,327 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6073:Cad
|
UTSW |
5 |
31,219,906 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6240:Cad
|
UTSW |
5 |
31,230,322 (GRCm39) |
missense |
probably benign |
0.00 |
R6260:Cad
|
UTSW |
5 |
31,224,144 (GRCm39) |
missense |
probably null |
|
R7145:Cad
|
UTSW |
5 |
31,224,956 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7303:Cad
|
UTSW |
5 |
31,217,557 (GRCm39) |
critical splice donor site |
probably null |
|
R7352:Cad
|
UTSW |
5 |
31,215,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R7382:Cad
|
UTSW |
5 |
31,233,173 (GRCm39) |
missense |
probably benign |
|
R7387:Cad
|
UTSW |
5 |
31,219,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R7455:Cad
|
UTSW |
5 |
31,231,506 (GRCm39) |
missense |
probably damaging |
0.99 |
R7596:Cad
|
UTSW |
5 |
31,226,392 (GRCm39) |
missense |
probably benign |
|
R7627:Cad
|
UTSW |
5 |
31,217,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R7898:Cad
|
UTSW |
5 |
31,218,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R8022:Cad
|
UTSW |
5 |
31,226,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R8115:Cad
|
UTSW |
5 |
31,218,271 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8511:Cad
|
UTSW |
5 |
31,233,165 (GRCm39) |
missense |
probably benign |
0.00 |
R8523:Cad
|
UTSW |
5 |
31,215,450 (GRCm39) |
missense |
probably damaging |
0.98 |
R8690:Cad
|
UTSW |
5 |
31,232,500 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8697:Cad
|
UTSW |
5 |
31,231,945 (GRCm39) |
missense |
probably benign |
0.06 |
R8698:Cad
|
UTSW |
5 |
31,234,819 (GRCm39) |
missense |
probably benign |
|
R8699:Cad
|
UTSW |
5 |
31,233,605 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9262:Cad
|
UTSW |
5 |
31,225,009 (GRCm39) |
missense |
probably null |
|
R9272:Cad
|
UTSW |
5 |
31,218,576 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9287:Cad
|
UTSW |
5 |
31,230,000 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9314:Cad
|
UTSW |
5 |
31,234,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R9609:Cad
|
UTSW |
5 |
31,228,018 (GRCm39) |
critical splice donor site |
probably null |
|
R9665:Cad
|
UTSW |
5 |
31,229,703 (GRCm39) |
missense |
probably benign |
0.28 |
RF001:Cad
|
UTSW |
5 |
31,217,556 (GRCm39) |
critical splice donor site |
probably benign |
|
RF012:Cad
|
UTSW |
5 |
31,217,556 (GRCm39) |
critical splice donor site |
probably benign |
|
X0021:Cad
|
UTSW |
5 |
31,225,475 (GRCm39) |
missense |
probably null |
1.00 |
X0022:Cad
|
UTSW |
5 |
31,229,661 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Cad
|
UTSW |
5 |
31,232,472 (GRCm39) |
missense |
probably benign |
0.25 |
Z1177:Cad
|
UTSW |
5 |
31,225,765 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TTTGGAGCTGGTCACGATC -3'
(R):5'- AACAAAGCAGCCAGGTGTCC -3'
Sequencing Primer
(F):5'- ACGATCATCCGGCTGATTAC -3'
(R):5'- CCTGAGCTTGTTATACCAATTAGGG -3'
|
Posted On |
2021-04-30 |